Canonical Allele Identifier: CA1694873485
Gene:

Linked Data

dbSNP Id: rs1787244569

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24283830_24283838del , CM000669.2:g.24283830_24283838del GRCh38
NC_000007.13:g.24323449_24323457del , CM000669.1:g.24323449_24323457del GRCh37
NC_000007.12:g.24289974_24289982del NCBI36
NG_016148.1:g.4643_4651del

Transcript Alleles

HGVS Amino-acid change
XM_017012910.1:c.42-28139_42-28131del XP_016868399.1:n.42-28139_42-28131del
XM_017012911.1:c.42-28139_42-28131del XP_016868400.1:n.42-28139_42-28131del
XR_001745121.1:n.473+35519_473+35527del
XR_001745122.1:n.345-86809_345-86801del
XR_001745123.1:n.473+35519_473+35527del
XR_001745124.1:n.473+35519_473+35527del
XR_001745125.1:n.473+35519_473+35527del
XR_001745126.1:n.473+35519_473+35527del
XR_001745127.1:n.345-28139_345-28131del
XR_001745129.1:n.473+35519_473+35527del
XR_001745130.1:n.473+35519_473+35527del
XR_001745131.1:n.473+35519_473+35527del
XR_001745132.1:n.473+35519_473+35527del